Canonical Allele Identifier: CA2176996419

Gene: SCG3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51682027A= , CM000677.2:g.51682027A=	GRCh38
NC_000015.9:g.51974224A= , CM000677.1:g.51974224A=	GRCh37
NC_000015.8:g.49761516A=	NCBI36
NG_013214.1:g.5675A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000220478.8:c.82+190A= MANE Select	ENSP00000220478.3:n.82+190A=
ENST00000220478.7:c.82+190A=	ENSP00000220478.3:n.82+190A=
ENST00000542355.6:c.-562+190A=	ENSP00000445205.2:n.-562+190A=
ENST00000558709.1:c.-419+190A=	ENSP00000452745.1:n.-419+190A=
NM_001165257.1:c.-562+190A=	NP_001158729.1:n.-562+190A=
NM_013243.3:c.82+190A=	NP_037375.2:n.82+190A=
NM_013243.4:c.82+190A= MANE Select	NP_037375.2:n.82+190A=
NM_001165257.2:c.-562+190A=	NP_001158729.1:n.-562+190A=